1,944 research outputs found

    FUTURE PARTICIPATION IN THE CONSERVATION RESERVE PROGRAM IN NORTH DAKOTA

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    The purpose of this study was to gauge the impact of agriculture and energy policies on conservation practices through a survey of conservation reserve program (CRP) contract holders in a selected Prairie Pothole Region of North Dakota-Burleigh, Kidder, and Stutsman Counties. The survey results showed that 48% of respondents are considering returning CRP acres to annual crop production once the contract expires. The largest influence on post-CRP land use was the market prices for production of annual crops. Respondents also identified lack of knowledge of conservation programs as a large hurdle to participation. This may indicate a need for improved communication from program information sources such as the Farm Service Agency and the Natural Resource Conservation Service, from where most contract holders get their information. These findings also provide interesting insight into the motivation and decision-making process surrounding conservation programs, in particular continued participation in the CRP. By understanding the main motivation and considerations for conservation participation (market prices, cost-sharing opportunities, and expected cost of production), federal conservation programs will be able to maximize conservation efforts, which will benefit landowners and resources alike

    Targeting, deployment and loss-tolerance in Lanchester engagements

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    Existing Lanchester combat models focus on two force parameters: numbers (force size) and per-capita effectiveness (attrition rate). While these two parameters are central in projecting a battle’s outcome, there are other important factors that affect the battlefield: (1) targeting capability, the capacity to identify live enemy units and not dissipate fire on non-targets; (2) tactical restrictions preventing full deployment of forces; and (3) morale and tolerance of losses, the capacity to endure casualties. In the spirit of Lanchester theory, we derive, for the first time, force-parity equations for various combinations of these effects, and obtain general implications and trade-offs. We show that more units and better weapons (higher attrition rate) are preferred over improved targeting capability and relaxed deployment restrictions unless these are poor. However, when facing aimed fire and unable to deploy more than half one’s force it is better to be able to deploy more existing units than to have either additional reserve units or the same increase in attrition effectiveness. Likewise more relaxed deployment constraints are preferred over enhanced loss-tolerance when initial reserves are greater than the force level at which withdrawal occurs

    OH yields from the CH3CO+O-2 reaction using an internal standard

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    Laser flash photolysis of CH3C(O)OH at 248 nm was used to create equal zero time yields of CH3CO and OH. The absolute OH yield from the CH3CO + O2 (+M) reaction was determined by following the OH temporal profile using the zero time OH concentration as an internal standard. The OH yield from CH3CO + O2 (+M) was observed to decrease with increasing pressure with an extrapolated zero pressure yield close to unity (1.1 ± 0.2, quoted uncertainties correspond to 95% confidence limits). The results are in quantitative agreement with those obtained from 248 nm acetone photolysis in the presence of O2

    Overusage of Mouse DH Gene Segment, DFL16.1, Is Strain-Dependent and Determined by cis-Acting Elements

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    The DJH structure is of particular importance for diversity in the immunoglobulin heavy chain because it encodes most of CDR3. Here, we investigate mechanisms responsible for generating the DJH structure. We found DFL16.1 was used at a high frequency in normal and transformed pre-B cells (fetal liver > 50%, A-MuLV lines ≅ 25%). One DFL16.1JH1 structure was found repeatedly and was also present in DJH and VDJH databases, suggesting this structure may be conserved in the primary repertoire. Genetic analysis demonstrated that C57BL/6 mice use DFL16.1 in DJH structures more frequently than BALB/c. Examination of individual alleles in (C57BL/6 BALB/c)F1 A-MuLV cell lines revealed that the C57BL/6-derived allele used DFL16.1 twice as often as the BALB/c. This result indicates that part of the mechanism ensuring overusage of DFL16.1 gene segments is cis-acting

    Objectively assessed physical activity and sedentary behaviour during pregnancy in portuguese women:Differences between trimesters and weekdays and weekends

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    Background: Engaging in physical activity (PA) and reducing sedentary behaviour (SB) are important for health during pregnancy, yet relatively few studies have examined these variables using objective measures and across trimesters during pregnancy. Objective: To determine the amount of objectively assessed PA and SB engaged in whether there was any weekday to weekend day variation in PA and SB during the first and second trimester of pregnancy. Method: PA and SB were determined using accelerometry worn over 7 consecutive days during each trimester in 137 Portuguese females (mean age ± SD = 29.6 ± 5.7). Results: In regard to the proportion of participants meeting the ACSM guidelines for PA, 37.5% of the participants in the first trimester and 29.6% of participants in the second trimester met the cut off of 30min or more of any type of moderate intensity activity on most (5) days of the week. Moderate intensity PA was significantly lower in trimester 2 compared to trimester 1 (P = 0.003). Moderate intensity PA was also significantly lower during weekends compared to weekdays irrespective of trimester (P = 0.003). SB, light and vigorous intensity PA were relatively stable from trimester 1 to trimester 2 and between weekdays and weekends (P < 0.05). Conclusion: The present study suggests that the majority of women do not meet PA guidelines for health during pregnancy and that moderate intensity PA declines form trimester 1 to 2 and is lower at weekends

    Effects of traumatic brain injury on cognitive functioning and cerebral metabolites in HIV-infected individuals.

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    We explored the possible augmenting effect of traumatic brain injury (TBI) history on HIV (human immunodeficiency virus) associated neurocognitive complications. HIV-infected participants with self-reported history of definite TBI were compared to HIV patients without TBI history. Groups were equated for relevant demographic and HIV-associated characteristics. The TBI group evidenced significantly greater deficits in executive functioning and working memory. N-acetylaspartate, a putative marker of neuronal integrity, was significantly lower in the frontal gray matter and basal ganglia brain regions of the TBI group. Together, these results suggest an additional brain impact of TBI over that from HIV alone. One clinical implication is that HIV patients with TBI history may need to be monitored more closely for increased risk of HIV-associated neurocognitive disorder signs or symptoms

    Through-life NEC scenario development

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    Scenarios are an important planning tool used by individuals, businesses and governments (especially in the military domain), but many of the currently used approaches focus solely on acute probabilistic timeframes and specific metricated instances of possible future states. Using a mixed method research methodology, we develop a scenario approach in which multiple timeframes are accommodated by fitting vignettes within each other to represent different time levels. This has the advantage of presenting the end-to-end process of capability development and instantiation. We describe the methodology employed to generate such a scenario as a demonstration aid for a large, multidisciplinary research program in systems of systems engineering. The process of scenario generation was an effective integration tool within this program (that included twelve distributed research groups). The resultant scenario enabled engagement of multiple stakeholders in an integrated demonstration of systems related research outputs. We recommend a new class of scenario (a “research scenario”) for incorporation within the standard classifications of scenario types

    Antithymocyte Globulin Plus G-CSF Combination Therapy Leads to Sustained Immunomodulatory and Metabolic Effects in a Subset of Responders With Established Type 1 Diabetes.

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    Low-dose antithymocyte globulin (ATG) plus pegylated granulocyte colony-stimulating factor (G-CSF) preserves β-cell function for at least 12 months in type 1 diabetes. Herein, we describe metabolic and immunological parameters 24 months following treatment. Patients with established type 1 diabetes (duration 4-24 months) were randomized to ATG and pegylated G-CSF (ATG+G-CSF) (N = 17) or placebo (N = 8). Primary outcomes included C-peptide area under the curve (AUC) following a mixed-meal tolerance test (MMTT) and flow cytometry. "Responders" (12-month C-peptide ≥ baseline), "super responders" (24-month C-peptide ≥ baseline), and "nonresponders" (12-month C-peptide &lt; baseline) were evaluated for biomarkers of outcome. At 24 months, MMTT-stimulated AUC C-peptide was not significantly different in ATG+G-CSF (0.49 nmol/L/min) versus placebo (0.29 nmol/L/min). Subjects treated with ATG+G-CSF demonstrated reduced CD4+ T cells and CD4+/CD8+ T-cell ratio and increased CD16+CD56hi natural killer cells (NK), CD4+ effector memory T cells (Tem), CD4+PD-1+ central memory T cells (Tcm), Tcm PD-1 expression, and neutrophils. FOXP3+Helios+ regulatory T cells (Treg) were elevated in ATG+G-CSF subjects at 6, 12, and 18 but not 24 months. Immunophenotyping identified differential HLA-DR expression on monocytes and NK and altered CXCR3 and PD-1 expression on T-cell subsets. As such, a group of metabolic and immunological responders was identified. A phase II study of ATG+G-CSF in patients with new-onset type 1 diabetes is ongoing and may support ATG+G-CSF as a prevention strategy in high-risk subjects

    Secreted NS1 of Dengue Virus Attaches to the Surface of Cells via Interactions with Heparan Sulfate and Chondroitin Sulfate E

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    Dengue virus (DENV) nonstructural protein-1 (NS1) is a secreted glycoprotein that is absent from viral particles but accumulates in the supernatant and on the plasma membrane of cells during infection. Immune recognition of cell surface NS1 on endothelial cells has been hypothesized as a mechanism for the vascular leakage that occurs during severe DENV infection. However, it has remained unclear how NS1 becomes associated with the plasma membrane, as it contains no membrane-spanning sequence motif. Using flow cytometric and ELISA-based binding assays and mutant cell lines lacking selective glycosaminoglycans, we show that soluble NS1 binds back to the surface of uninfected cells primarily via interactions with heparan sulfate and chondroitin sulfate E. DENV NS1 binds directly to the surface of many types of epithelial and mesenchymal cells yet attaches poorly to most peripheral blood cells. Moreover, DENV NS1 preferentially binds to cultured human microvascular compared to aortic or umbilical cord vein endothelial cells. This binding specificity was confirmed in situ as DENV NS1 bound to lung and liver but not intestine or brain endothelium of mouse tissues. Differential binding of soluble NS1 by tissue endothelium and subsequent recognition by anti-NS1 antibodies could contribute to the selective vascular leakage syndrome that occurs during severe secondary DENV infection
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